M Patterson

619 citations

27 papers · 505 indexed · h-index 12

Impact in

Genetics top 2%
- Hemoglobinopathies and Related Disorders
Hematology top 5%
- Iron Metabolism and Disorders
- Blood groups and transfusion

Papers in

Genetics 21
- Hemoglobinopathies and Related Disorders 21
Hematology 13
- Iron Metabolism and Disorders 10
- Blood groups and transfusion 2

Co-authors: David H.K. Chui Barry Eng Jack Gauldie Timothy W. Brotherton John S. Waye DR Higgs L. Walker L. R. Walker
Journals: Blood (6 papers)Annals of the New York Academy of Sciences (2 papers)Proceedings of the National Academy of Sciences (2 papers)Hemoglobin (15 papers)Medical Physics (1 paper)
Partner nations: Canada United States Netherlands

In The Last Decade

M Patterson

26 papers receiving 482 citations

Peers

Countries citing papers authored by M Patterson

Since Specialization

Citations

This map shows the geographic impact of M Patterson's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by M Patterson with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites M Patterson more than expected).

Fields of papers citing papers by M Patterson

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by M Patterson. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by M Patterson. The network helps show where M Patterson may publish in the future.

Co-authorship network

The 25 scholars most cited alongside M Patterson, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with M Patterson Line = papers co-authored together M Patterson links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	SU‐E‐T‐34: Time Series Analysis of Skin Reactions during Heck and Neck IMRT Medical Physics ·Xiangru Tang, Raymond David Hager, Tian Guiyun, M Patterson, Joseph E. Hayward, Theo Farrell	2011	1
2	Three New α-Thalassemia Point Mutations Ascertained Through Newborn Screening Hemoglobin ·Barry Eng, M Patterson, L. R. Walker, Carolyn Hoppe, Mahin Azimi, Helen Lee, Piero C. Giordano, John S. Waye	2006	10
3	High Hb A₂β-Thalassemia Due to a 468 bp Deletion in a Patient with Hb S/β-Thalassemia Hemoglobin ·M Patterson, L. R. Walker, Barry Eng, John S. Waye	2005	3
4	Prenatal Diagnosis of Hemoglobinopathies in Ontario, Canada Annals of the New York Academy of Sciences ·Raveen Basran, M Patterson, L. R. Walker, Edouardo Bintang Rokatenda, Barry Eng, David H.K. Chui, John S. Waye	2005	13
5	Characterization of a Rare Single α-Globin Gene Deletion in a Chinese Woman with Hb H Disease Hemoglobin ·Barry Eng, Jennifer Elizabeth McMullen, L. R. Walker, M Patterson, John S. Waye	2005	11
6	Identification of a New δ Chain Hemoglobin Variant in a β-Thalassemia Carrier: Hb A₂-MUMC [δ13(A10)Ala → Asp] Hemoglobin ·L. R. Walker, M Patterson, Barry Eng, Foziyeh Khodadadi, John S. Waye	2005	1
7	Hb Castilla [β32(B14)Leu → Arg] Caused by a De Novo Mutation Hemoglobin ·L. R. Walker, Foziyeh Khodadadi, M Patterson, Barry Eng, John S. Waye	2003	1
8	Identification of a New β-Thalassemia Nonsense Mutation [Codon 59 (AAG→TAG)] Hemoglobin ·M Patterson, L. R. Walker, David H.K. Chui, Alan R. Cohen, John S. Waye	2003	8
9	Identification of a new hemoglobin variant: Hb St. Joseph's [β77(EF1)His→Leu] Hemoglobin ·M Patterson, L. R. Walker, David H.K. Chui, John Lafferty, Vicente Curiel JM, John S. Waye	2003	1
10	Detection of Severe Nondeletional α -Thalassemia Mutations Using a Single-Tube Multiplex ARMS Assay Genetic Testing ·Barry Eng, M Patterson, L. Walker, David H.K. Chui, John S. Waye	2001	50
11	NOVEL β-THALASSEMIA MUTATION IN A β-THALASSEMIA INTERMEDIA PATIENT [POLY A (AATAAA →GATAAA)] Hemoglobin ·John S. Waye, Barry Eng, M Patterson, Marciano D. Reis, 淳亀井, David H.K. Chui	2001	5
12	Compound Heterozygosity for Hb S and Hb G-Copenhagen Hemoglobin ·Manuel Carção, L. Chang, Annette Poon, Nancy F. Olivieri, John S. Waye, Barry Eng, M Patterson, David H.K. Chui	1999	0
13	Spectrum of β-Thalassemia Mutations in Egypt Hemoglobin ·John S. Waye, G. H. Hogeboom, Barry Eng, M Patterson, David H.K. Chui, R.F. Grol, Fan Liang, Zeinab Afify	1999	16
14	Novel β-Thalassemia Mutation In Patients of Jewish Descent: [β30(B12)ARGGLY OR IVS-I (-2) (AG)] Hemoglobin ·John S. Waye, Barry Eng, M Patterson, David H.K. Chui, J. Fernandes	1998	8
15	Novel β°-Thalassemia Mutation in a Canadian Woman of British Descent (Codons 72/73, -Agtga, +T) Hemoglobin ·John S. Waye, Barry Eng, M Patterson, David H.K. Chui, J. Fernandes	1997	3
16	Novel Mutation of the α2-Globin Gene Initiation Codon (Atg→A-G) in a Vietnamese Girl with Hb H Disease Hemoglobin ·John S. Waye, Barry Eng, M Patterson, David H.K. Chui, Eric Nisbet‐Brown, Nancy F. Olivieri	1997	10
17	Identifican of A New High Oxygen Affinity Hemoglobin Variant: Hb Aurora [β139(H17)Asn→Tyr] Hemoglobin ·John Lafferty, Mahmoud Ali, Srijita Chakraborti, Barry Eng, M Patterson, John S. Waye	1995	6
18	De novoβ-globin gene mutation [β63(E7)HIS→TYR] giving rise to Hb M disease in a newfoundlander Hemoglobin ·John S. Waye, M Patterson, Barry Eng	1994	4
19	Identification of a novel termination codon mutation (TAA-->TAT, Term-- >Tyr) in the alpha 2 globin gene of a Laotian girl with hemoglobin H disease [letter] Blood ·Goia, Barry Eng, M Patterson, David H.K. Chui, Timothy Hawes	1994	30
20	Human embryonic zeta-globin chains in fetal and newborn blood Blood ·David H.K. Chui, W C Mentzer, M Patterson, Cristian Zeno Mihiţ, Cornelis Dekramer, Lisa Rene Vickers, Yen-Ting Chou, DR Higgs	1989	26

About M Patterson

M Patterson is a scholar working on Genetics, Hematology, Pediatrics, Perinatology and Child Health, Rheumatology and Physiology, having authored 27 papers that have together received 505 indexed citations. Recurring topics across this work include Hemoglobinopathies and Related Disorders (21 papers), Iron Metabolism and Disorders (10 papers), Erythrocyte Function and Pathophysiology (5 papers), Neonatal Health and Biochemistry (3 papers), Folate and B Vitamins Research (3 papers), Cystic Fibrosis Research Advances (2 papers), Blood groups and transfusion (2 papers) and Prenatal Screening and Diagnostics (2 papers). The work is most often cited by research in Genetics (359 citations), Hematology (262 citations), Physiology (163 citations), Cell Biology (84 citations) and Pediatrics, Perinatology and Child Health (90 citations). M Patterson has collaborated with scholars based in Canada, United States and Netherlands. Frequent co-authors include David H.K. Chui, Barry Eng, Jack Gauldie, Timothy W. Brotherton, John S. Waye, DR Higgs, L. Walker, L. R. Walker, Murray Enkin and NF Olivieri. Their work appears in journals such as Blood, Annals of the New York Academy of Sciences, Proceedings of the National Academy of Sciences, Hemoglobin and Medical Physics.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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